| Descriptor English: | WAGR Syndrome | ||||||
| Descriptor Spanish: |
Síndrome WAGR
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| Descriptor Portuguese: | Síndrome WAGR | ||||||
| Descriptor French: | Syndrome WAGR | ||||||
| Entry term(s): |
11p Partial Monosomy Syndrome Chromosome 11p13 Deletion Syndrome Complex, WAGR Contiguous Gene Syndrome, WAGR Syndrome, WAGR WAGR Complex WAGR Complices WAGR Contiguous Gene Syndrome WAGR Syndromes Wilms Tumor, Aniridia, Genitourinary Anomalies, And Mental Retardation Syndrome Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation Syndrome Wilms Tumor-Aniridia-Genital Anomalies-Retardation Syndrome Wilms Tumor-Aniridia-Genitourinary Anomalies-MR Syndrome Wilms Tumor-Aniridia-Gonadoblastoma-Mental Retardation Syndrome |
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| Tree number(s): |
C04.557.435.595.950 C04.588.945.947.535.585.950 C04.700.900.950 C10.597.606.360.969 C11.250.060.950 C11.270.060.950 C11.941.375.060.950 C12.050.351.875.253.096.875 C12.050.351.937.820.535.585.950 C12.050.351.968.419.473.585.950 C12.200.706.316.096.875 C12.200.758.820.750.585.950 C12.200.777.419.473.585.950 C12.800.316.096.875 C12.900.820.535.585.950 C12.950.419.473.585.950 C12.950.983.535.585.950 C16.131.260.940 C16.131.384.079.950 C16.131.939.316.096.875 C16.320.180.940 C16.320.290.078.950 C16.320.700.900.950 C19.391.119.096.875 |
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| RDF Unique Identifier: | https://id.nlm.nih.gov/mesh/D017624 | ||||||
| Scope note: | A contiguous gene syndrome associated with hemizygous deletions of chromosome region 11p13. The condition is marked by the combination of WILMS TUMOR; ANIRIDIA; GENITOURINARY ABNORMALITIES; and INTELLECTUAL DISABILITY. |
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| Allowable Qualifiers: |
BL blood CF cerebrospinal fluid CI chemically induced CL classification CO complications DG diagnostic imaging DH diet therapy DI diagnosis DT drug therapy EC economics EH ethnology EM embryology EN enzymology EP epidemiology ET etiology GE genetics HI history IM immunology ME metabolism MI microbiology MO mortality NU nursing PA pathology PC prevention & control PP physiopathology PS parasitology PX psychology RH rehabilitation RT radiotherapy SU surgery TH therapy UR urine VE veterinary VI virology |
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| Previous Indexing: |
Chromosomes, Human, 6-12 (1980-1985) Chromosomes, Human, Pair 11 (1986-1993) Iris/abnormalities (1980-1993) Mental Retardation (1984-1993) Nephroblastoma (1980-1993) Urogenital System/abnormalities (1984-1993) |
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| Public MeSH Note: | 1994 |
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| History Note: | 1994 |
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| Related: |
Genes, Wilms Tumor
MeSH | ||||||
| DeCS ID: | 30974 | ||||||
| Unique ID: | D017624 | ||||||
| Documents indexed in the Virtual Health Library (VHL): | Click here to access the VHL documents | ||||||
| Date Established: | 1994/01/01 | ||||||
| Date of Entry: | 1993/06/03 | ||||||
| Revision Date: | 2018/06/29 |
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DISEASES
Neoplasms [C04]Neoplasms -
DISEASES
Neoplasms [C04]Neoplasms -
DISEASES
Neoplasms [C04]Neoplasms -
DISEASES
Eye Diseases [C11]Eye Diseases -
DISEASES
Eye Diseases [C11]Eye Diseases -
DISEASES
Eye Diseases [C11]Eye Diseases
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WAGR Syndrome
- Preferred
| Concept UI |
M0026692 |
| Scope note | A contiguous gene syndrome associated with hemizygous deletions of chromosome region 11p13. The condition is marked by the combination of WILMS TUMOR; ANIRIDIA; GENITOURINARY ABNORMALITIES; and INTELLECTUAL DISABILITY. |
| Preferred term | WAGR Syndrome |
| Entry term(s) |
11p Partial Monosomy Syndrome Chromosome 11p13 Deletion Syndrome Complex, WAGR Contiguous Gene Syndrome, WAGR Syndrome, WAGR WAGR Complex WAGR Complices WAGR Contiguous Gene Syndrome WAGR Syndromes Wilms Tumor, Aniridia, Genitourinary Anomalies, And Mental Retardation Syndrome Wilms Tumor, Aniridia, Genitourinary Anomalies, Mental Retardation Syndrome Wilms Tumor-Aniridia-Genital Anomalies-Retardation Syndrome Wilms Tumor-Aniridia-Genitourinary Anomalies-MR Syndrome Wilms Tumor-Aniridia-Gonadoblastoma-Mental Retardation Syndrome |
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